Allele Registry

Canonical Allele Identifier: PA2827773559

Gene: SCN1A HGNC NCBI

ClinVar RCV:

RCV000059478

RCV000519717

RCV003992313

ClinVar Variation:

68601

451108

HGVS (amino-acid)	Matching Registered Transcripts
NP_001340881.1:p.His928Gln	CA285090 NM_001353952.2:c.2784C>G CA349061306 NM_001353952.2:c.2784C>A